Cargando…

IgG4-Related Disease: Dataset of 235 Consecutive Patients

Immunoglobulin G4-related disease (IgG4-RD) is a recently discovered systemic condition, in which various organ manifestations are linked by a similar histological appearance. Our knowledge of this condition is still fragmented, as most studies have examined only a few dozen patients or focused on a...

Descripción completa

Detalles Bibliográficos
Autores principales: Inoue, Dai, Yoshida, Kotaro, Yoneda, Norihide, Ozaki, Kumi, Matsubara, Takashi, Nagai, Keiichi, Okumura, Kenichirou, Toshima, Fumihito, Toyama, Jun, Minami, Tetsuya, Matsui, Osamu, Gabata, Toshifumi, Zen, Yoh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602507/
https://www.ncbi.nlm.nih.gov/pubmed/25881845
http://dx.doi.org/10.1097/MD.0000000000000680
_version_ 1782394733525467136
author Inoue, Dai
Yoshida, Kotaro
Yoneda, Norihide
Ozaki, Kumi
Matsubara, Takashi
Nagai, Keiichi
Okumura, Kenichirou
Toshima, Fumihito
Toyama, Jun
Minami, Tetsuya
Matsui, Osamu
Gabata, Toshifumi
Zen, Yoh
author_facet Inoue, Dai
Yoshida, Kotaro
Yoneda, Norihide
Ozaki, Kumi
Matsubara, Takashi
Nagai, Keiichi
Okumura, Kenichirou
Toshima, Fumihito
Toyama, Jun
Minami, Tetsuya
Matsui, Osamu
Gabata, Toshifumi
Zen, Yoh
author_sort Inoue, Dai
collection PubMed
description Immunoglobulin G4-related disease (IgG4-RD) is a recently discovered systemic condition, in which various organ manifestations are linked by a similar histological appearance. Our knowledge of this condition is still fragmented, as most studies have examined only a few dozen patients or focused on a particular organ manifestation. This study was conducted to learn the demography and patient characteristics of IgG4-RD using a large cohort. A total of 235 consecutive patients with IgG4-RD, diagnosed in 8 general hospitals in the same medical district, were identified by searching the institutions’ radiology database. Inclusion criteria were histology-proven IgG4-RD according to the Pathology Consensus Statement and/or definitive type 1 autoimmune pancreatitis meeting the International Consensus Diagnostic Criteria. Clinical notes and images of selected patients were retrospectively reviewed. All patients were adults (M/F = 4/1). The median age was 67 years (range 35–86). Nine tenths were diagnosed in their 50s to 70s. Among 486 manifestations identified in total, the most common was pancreatitis diagnosed in 142 patients (60%), followed by sialadenitis (34%), tubulointerstitial nephritis (23%), dacryoadenitis (23%), and periaortitis (20%). The majority of patients (95%) had at least 1 of the 5 most common manifestations. Male and female patients differed in their organ manifestations (periaortitis more common in males and sialodacryoadenitis more common in females). Serum IgG4 (normal ≤135 mg/dL) was elevated to >135 mg/dL in 208 patients (88%) and >270 mg/dL in 167 (71%). The IgG4 value was significantly higher in patients with multiorgan involvement than in those with a single manifestation (median 629 mg/dL vs 299 mg/dL, P < 0.01). Of 218 patients, for whom both IgG4 and IgG values were available, the IgG4/IgG ratio was raised to >10% in 194 (89%). Corticosteroids were effective, but the relapse rate was estimated to be 24% in the study period (median 37 months). During the follow-up, 15 malignant diseases were diagnosed in 13 patients (6%). This figure is similar to the incidence (12.9 cancers) expected from the Japanese nationwide study for cancer epidemiology (standardized incidence ratio 1.16). In conclusion, this reliable dataset could improve the characterization of IgG4-RD, particularly its unique demography and the frequency of each organ manifestation.
format Online
Article
Text
id pubmed-4602507
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-46025072015-10-27 IgG4-Related Disease: Dataset of 235 Consecutive Patients Inoue, Dai Yoshida, Kotaro Yoneda, Norihide Ozaki, Kumi Matsubara, Takashi Nagai, Keiichi Okumura, Kenichirou Toshima, Fumihito Toyama, Jun Minami, Tetsuya Matsui, Osamu Gabata, Toshifumi Zen, Yoh Medicine (Baltimore) 3600 Immunoglobulin G4-related disease (IgG4-RD) is a recently discovered systemic condition, in which various organ manifestations are linked by a similar histological appearance. Our knowledge of this condition is still fragmented, as most studies have examined only a few dozen patients or focused on a particular organ manifestation. This study was conducted to learn the demography and patient characteristics of IgG4-RD using a large cohort. A total of 235 consecutive patients with IgG4-RD, diagnosed in 8 general hospitals in the same medical district, were identified by searching the institutions’ radiology database. Inclusion criteria were histology-proven IgG4-RD according to the Pathology Consensus Statement and/or definitive type 1 autoimmune pancreatitis meeting the International Consensus Diagnostic Criteria. Clinical notes and images of selected patients were retrospectively reviewed. All patients were adults (M/F = 4/1). The median age was 67 years (range 35–86). Nine tenths were diagnosed in their 50s to 70s. Among 486 manifestations identified in total, the most common was pancreatitis diagnosed in 142 patients (60%), followed by sialadenitis (34%), tubulointerstitial nephritis (23%), dacryoadenitis (23%), and periaortitis (20%). The majority of patients (95%) had at least 1 of the 5 most common manifestations. Male and female patients differed in their organ manifestations (periaortitis more common in males and sialodacryoadenitis more common in females). Serum IgG4 (normal ≤135 mg/dL) was elevated to >135 mg/dL in 208 patients (88%) and >270 mg/dL in 167 (71%). The IgG4 value was significantly higher in patients with multiorgan involvement than in those with a single manifestation (median 629 mg/dL vs 299 mg/dL, P < 0.01). Of 218 patients, for whom both IgG4 and IgG values were available, the IgG4/IgG ratio was raised to >10% in 194 (89%). Corticosteroids were effective, but the relapse rate was estimated to be 24% in the study period (median 37 months). During the follow-up, 15 malignant diseases were diagnosed in 13 patients (6%). This figure is similar to the incidence (12.9 cancers) expected from the Japanese nationwide study for cancer epidemiology (standardized incidence ratio 1.16). In conclusion, this reliable dataset could improve the characterization of IgG4-RD, particularly its unique demography and the frequency of each organ manifestation. Wolters Kluwer Health 2015-04-17 /pmc/articles/PMC4602507/ /pubmed/25881845 http://dx.doi.org/10.1097/MD.0000000000000680 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 3600
Inoue, Dai
Yoshida, Kotaro
Yoneda, Norihide
Ozaki, Kumi
Matsubara, Takashi
Nagai, Keiichi
Okumura, Kenichirou
Toshima, Fumihito
Toyama, Jun
Minami, Tetsuya
Matsui, Osamu
Gabata, Toshifumi
Zen, Yoh
IgG4-Related Disease: Dataset of 235 Consecutive Patients
title IgG4-Related Disease: Dataset of 235 Consecutive Patients
title_full IgG4-Related Disease: Dataset of 235 Consecutive Patients
title_fullStr IgG4-Related Disease: Dataset of 235 Consecutive Patients
title_full_unstemmed IgG4-Related Disease: Dataset of 235 Consecutive Patients
title_short IgG4-Related Disease: Dataset of 235 Consecutive Patients
title_sort igg4-related disease: dataset of 235 consecutive patients
topic 3600
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602507/
https://www.ncbi.nlm.nih.gov/pubmed/25881845
http://dx.doi.org/10.1097/MD.0000000000000680
work_keys_str_mv AT inouedai igg4relateddiseasedatasetof235consecutivepatients
AT yoshidakotaro igg4relateddiseasedatasetof235consecutivepatients
AT yonedanorihide igg4relateddiseasedatasetof235consecutivepatients
AT ozakikumi igg4relateddiseasedatasetof235consecutivepatients
AT matsubaratakashi igg4relateddiseasedatasetof235consecutivepatients
AT nagaikeiichi igg4relateddiseasedatasetof235consecutivepatients
AT okumurakenichirou igg4relateddiseasedatasetof235consecutivepatients
AT toshimafumihito igg4relateddiseasedatasetof235consecutivepatients
AT toyamajun igg4relateddiseasedatasetof235consecutivepatients
AT minamitetsuya igg4relateddiseasedatasetof235consecutivepatients
AT matsuiosamu igg4relateddiseasedatasetof235consecutivepatients
AT gabatatoshifumi igg4relateddiseasedatasetof235consecutivepatients
AT zenyoh igg4relateddiseasedatasetof235consecutivepatients